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Front Mol Biosci. 2018 Jan 17;4:100. doi: 10.3389/fmolb.2017.00100. eCollection 2017.
2
Crystal structure of the adenosine A receptor bound to an antagonist reveals a potential allosteric pocket.与拮抗剂结合的腺苷A受体的晶体结构揭示了一个潜在的变构口袋。
Proc Natl Acad Sci U S A. 2017 Feb 21;114(8):2066-2071. doi: 10.1073/pnas.1621423114. Epub 2017 Feb 6.
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Application of Strep-Tactin XT for affinity purification of Twin-Strep-tagged CB, a G protein-coupled cannabinoid receptor.链霉抗生物素蛋白XT在亲和纯化双Strep标签的CB(一种G蛋白偶联大麻素受体)中的应用。
Protein Expr Purif. 2017 Mar;131:109-118. doi: 10.1016/j.pep.2016.11.006. Epub 2016 Nov 17.
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Crystal structures of the M1 and M4 muscarinic acetylcholine receptors.M1和M4毒蕈碱型乙酰胆碱受体的晶体结构。
Nature. 2016 Mar 17;531(7594):335-40. doi: 10.1038/nature17188. Epub 2016 Mar 9.
5
Development of the Twin-Strep-tag® and its application for purification of recombinant proteins from cell culture supernatants.双Strep标签的开发及其在从细胞培养上清液中纯化重组蛋白的应用
Protein Expr Purif. 2013 Nov;92(1):54-61. doi: 10.1016/j.pep.2013.08.021. Epub 2013 Sep 6.
6
Global fold of human cannabinoid type 2 receptor probed by solid-state 13C-, 15N-MAS NMR and molecular dynamics simulations.固态 13C-、15N-MAS NMR 和分子动力学模拟探测人类大麻素型 2 受体的全局折叠。
Proteins. 2014 Mar;82(3):452-65. doi: 10.1002/prot.24411. Epub 2013 Oct 17.
7
A brief history of G-protein coupled receptors (Nobel Lecture).G蛋白偶联受体简史(诺贝尔演讲)
Angew Chem Int Ed Engl. 2013 Jun 17;52(25):6366-78. doi: 10.1002/anie.201301924. Epub 2013 May 6.
8
Efficient isotopic tryptophan labeling of membrane proteins by an indole controlled process conduct.吲哚控制过程促进的膜蛋白高效同位素色氨酸标记。
Biotechnol Bioeng. 2013 Jun;110(6):1681-90. doi: 10.1002/bit.24830. Epub 2013 Jan 17.
9
Structure of the chemokine receptor CXCR1 in phospholipid bilayers.化学趋化因子受体 CXCR1 在磷脂双层中的结构。
Nature. 2012 Nov 29;491(7426):779-83. doi: 10.1038/nature11580. Epub 2012 Oct 21.
10
Stabilization of functional recombinant cannabinoid receptor CB(2) in detergent micelles and lipid bilayers.功能重组大麻素受体 CB(2)在去污剂胶束和脂质双层中的稳定化。
PLoS One. 2012;7(10):e46290. doi: 10.1371/journal.pone.0046290. Epub 2012 Oct 3.

用于核磁共振结构研究的G蛋白偶联大麻素受体CB的表达与制备

Expression and Preparation of a G-Protein-Coupled Cannabinoid Receptor CB for NMR Structural Studies.

作者信息

Yeliseev Alexei

机构信息

National Institute on Alcoholism and Alcohol Abuse, National Institutes of Health, Rockville, Maryland.

出版信息

Curr Protoc Protein Sci. 2019 Jun;96(1):e83. doi: 10.1002/cpps.83. Epub 2019 Jan 9.

DOI:10.1002/cpps.83
PMID:30624864
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6579622/
Abstract

Cannabinoid receptor type II, or CB , is an integral membrane protein that belongs to a large class of G-protein-coupled receptors (GPCR)s. CB is a part of the endocannabinoid system, which plays an important role in the regulation of immune response, inflammation, and pain. Information about the structure and function of CB is essential for the development of specific ligands targeting this receptor. We present here a methodology for recombinant expression of CB and its stable isotope labeling, purification, and reconstitution into liposomes, in preparation for its characterization by nuclear magnetic resonance (NMR). Correctly folded, functional CB labeled with [ C, N]tryptophan or uniformly labeled with C and N is expressed in a medium of defined composition, under controlled aeration, pH, and temperature conditions. The receptor is purified by affinity chromatography and reconstituted into lipid bilayers in the form of proteoliposomes suitable for analysis by NMR spectroscopy. © 2019 by John Wiley & Sons, Inc.

摘要

II型大麻素受体,即CB₂,是一种整合膜蛋白,属于一大类G蛋白偶联受体(GPCR)。CB₂是内源性大麻素系统的一部分,该系统在免疫反应、炎症和疼痛的调节中发挥重要作用。有关CB₂结构和功能的信息对于开发靶向该受体的特异性配体至关重要。我们在此介绍一种用于CB₂重组表达及其稳定同位素标记、纯化并重构到脂质体中的方法,为通过核磁共振(NMR)对其进行表征做准备。用[¹³C,¹⁵N]色氨酸标记或用¹³C和¹⁵N均匀标记的正确折叠的功能性CB₂,在确定组成的培养基中,在受控的通气、pH和温度条件下表达。该受体通过亲和色谱法纯化,并重构为适合核磁共振光谱分析的蛋白脂质体形式的脂质双层。© 2019约翰威立父子出版公司